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ammosamide a

Description

ammosamide A: structure in first source [MeSH]

Cross-References

ID SourceID
PubMed CID25172829
CHEMBL ID4100877
SCHEMBL ID261071
MeSH IDM0528859

Synonyms (4)

Synonym
SCHEMBL261071
ammosamide a
CHEMBL4100877
9,11-diamino-10-chloro-2-methyl-3-sulfanylidene-2,7-diazatricyclo[6.3.1.04,12]dodeca-1(11),4,6,8(12),9-pentaene-6-carboxamide

Bioassays (3)

Assay IDTitleYearJournalArticle
AID1437640Cytotoxicity against human HCT116 cells assessed as growth inhibition by MTS assay2017Journal of natural products, 01-27, Volume: 80, Issue:1
ISSN: 1520-6025
Thiol-Based Probe for Electrophilic Natural Products Reveals That Most of the Ammosamides Are Artifacts.
AID1437645Antibacterial activity against Escherichia coli MG1655 at 10 ug after 48 hrs by disk diffusion method2017Journal of natural products, 01-27, Volume: 80, Issue:1
ISSN: 1520-6025
Thiol-Based Probe for Electrophilic Natural Products Reveals That Most of the Ammosamides Are Artifacts.
AID1437641Cytotoxicity against human HCT116 cells assessed as growth inhibition at 78.125 ug/ml by MTS assay relative to control2017Journal of natural products, 01-27, Volume: 80, Issue:1
ISSN: 1520-6025
Thiol-Based Probe for Electrophilic Natural Products Reveals That Most of the Ammosamides Are Artifacts.

Research

Studies (7)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's2 (28.57)29.6817
2010's5 (71.43)24.3611
2020's0 (0.00)2.80

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other7 (100.00%)84.16%
SubstanceStudiesClassesRolesFirst YearLast YearAverage AgeRelationship StrengthTrialspre-19901990's2000's2010'spost-2020
etoposidebeta-D-glucoside;
furonaphthodioxole;
organic heterotetracyclic compound
antineoplastic agent;
DNA synthesis inhibitor
201720177.0low000010
ammosamide b201720177.0medium000010
SubstanceStudiesClassesRolesFirst YearLast YearAverage AgeRelationship StrengthTrialspre-19901990's2000's2010'spost-2020
carbostyrilmonohydroxyquinoline;
quinolone
bacterial xenobiotic metabolite201620168.0low000010
pyrrolespyrrole;
secondary amine
201620168.0low000010
2-oxindolegamma-lactam;
indolinone
201620168.0low000010
pyrroloquinoline201620168.0low000010
ammosamide b2009201613.0high000420
ConditionIndicatedStudiesFirst YearLast YearAverage AgeRelationship StrengthTrialspre-19901990's2000's2010'spost-2020